CODMAN Craniotomy Kit - Indonesia BPOM Medical Device Registration
CODMAN Craniotomy Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002420090. The device is manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCountry of Origin
United States
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Foresta Business Loft 6 Unit 2, Jl. BSD Boulevard Utara, Kelurahan Lengkong Kulon, Kecamatan Pagedangan, Kabupaten Tangerang, Banten 15331, Indonesia
Registration Date
Oct 23, 2024
Expiry Date
Feb 13, 2029
Product Type
Surgical Neurology Equipment
Manual cranial drills, burrs, trephines, and their accessories
Non Electromedic Sterile
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